Sr. Clinical Research Associate (Romania)
Alimentiv · Bucharest
Clinical OperationsCompany career page
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Role summary
Senior Clinical Research Associate responsible for independent oversight of clinical site monitoring activities, ensuring protocol and regulatory compliance across investigative sites. Reports directly to sponsor and Alimentiv leadership while mentoring junior CRAs and collaborating across functional teams.
What they're looking for
- Proven experience as Clinical Research Associate or equivalent clinical operations role
- Demonstrated knowledge of ICH/GCP guidelines and clinical trial regulations
- Strong understanding of protocol compliance and regulatory documentation requirements
- Experience coordinating between sponsors and investigative sites
- Mentoring and leadership capabilities for junior-level staff
- Fluency in English; local language proficiency preferred
What you'll be doing
- Independently manage site monitoring activities and assess protocol compliance
- Serve as primary liaison between sponsor, Alimentiv, and investigative sites
- Mentor and provide guidance to CRA I and II level staff members
- Conduct CRA Assessment Visits and participate in audits or inspections as needed
- Collaborate with cross-functional stakeholders on clinical study execution
Privacy & handoff
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